Ignite Creation Date:
2024-05-06 @ 8:23 PM
Last Modification Date:
2024-10-26 @ 3:26 PM
Study NCT ID:
NCT06365710
Status:
RECRUITING
Last Update Posted:
2024-04-15
First Post:
2024-04-09
Brief Title:
Physiotherapy vs Telerehabilitation After Volar Plating of Distal Radius Fracture
Sponsor:
Töölö Hospital
Organization:
Töölö Hospital
Study Overview
Official Title:
A Randomized Controlled Trial Comparing Traditional Physiotherapy vs Telerehabilitation After Volar Plating of Distal Radius Fracture a Study Protocol
Status:
RECRUITING
Status Verified Date:
2024-04
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
Trial purpose is to research the outcome comparing traditional physiotherapy vs telerehabilitation after volar plating of distal radius fracture
Patients with distal radius fracture that meet the operative criteria set by the Finnish Current Care guidelines are randomized 11 computer generated sequence with random block size to two parallel groups and will undergo operative treatment and traditional physiotherapy vs telerehabilitation
Baseline data is collected preoperatively and patients are followed at 1 3 and 12 months after enrollment The primary end-point is 3 months and the primary outcome is the Patient-Rated Wrist Evaluation PRWE
Patients with distal radius fracture that meet the operative criteria set by the Finnish Current Care guidelines are randomized 11 computer generated sequence with random block size to two parallel groups and will undergo operative treatment and traditional physiotherapy vs telerehabilitation
Baseline data is collected preoperatively and patients are followed at 1 3 and 12 months after enrollment The primary end-point is 3 months and the primary outcome is the Patient-Rated Wrist Evaluation PRWE
Detailed Description:
None
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None